FDA UDI In Commercial Distribution 🇺🇸 United States

GORE® VIABAHN® FORTEGRA Venous Stent

DI: 00733132663972 · Model: VNS101502A · W. L. Gore & Associates, Inc.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
GORE® VIABAHN® FORTEGRA Venous Stent
Primary DI
00733132663972
Version / Model
VNS101502A
Catalog Number
VNS101502A
Company Name
W. L. Gore & Associates, Inc.
Labeler DUNS
967358115
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2026-01-08
Public Version
1
Public Version Date
2026-01-16
Public Version Status
New
Public Device Record Key
1a680989-2936-4f3a-b516-9c1a62c6b9b9

Device Description

FORTEGRA VENOUS STENT 10mm x 150mm

Device Characteristics

Single Use
Yes
Prescription Use (Rx)
Yes
Over the Counter (OTC)
No
Kit
No
Combination Product
No
HCT/P
No
Contains NRL
No
Not Made with NRL
No
MRI Safety
MR Conditional
Direct Marking Exempt
No
PM Exempt
No
Has Serial Number
Yes
Has Lot/Batch Number
No
Has Manufacturing Date
Yes
Has Expiration Date
Yes
Has Donation ID
No

Sterilization

Is Sterile
Yes
Sterilization Prior Use
No

Product Codes

Code Name
QTL Stent, Vena Cava

GMDN Terms

Code Name
67398 Polymer-coated central/peripheral venous stent

Identifiers

Type ID
Primary 00733132663972

Customer Contacts

Phone
800-528-8763

Premarket Submissions

Submission Number Supplement Number
P250017 000

Storage Conditions

Type
Handling Environment Temperature
Temperature Range
15 – 30 Degrees Celsius